[1]
Farjami, Z., Khodaienia, N., Ebrahimi, N., Zamani Ghaletaki, G.,  Ashnaei, A., Galehdari, M., Moradyar, M. and Houshmand, M. 2020. A case report of congenital myasthenic syndrome caused by a mutation in the CHRNE gene in the Iranian population. Iranian Journal of Child Neurology. 14, 4 (Oct. 2020), 87–94. DOI:https://doi.org/10.22037/ijcn.v14i4.20178.